Back to discover
Disease

congenital bilateral aplasia of vas deferens from CFTR mutation

Also known as CAVD, CBAVD, congenital bilateral absence of vas deferens, congenital bilateral aplasia of the vas deferens+1 more

CAVD, CBAVD, congenital bilateral absence of vas deferens, congenital bilateral aplasia of the vas deferens, vas deferens, congenital bilateral aplasia of.

2
Associated genes
1
Related proteins

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

No activity recorded in this window. Try a wider timeframe.

Associated genes

2 matches

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

CFTR0.82ADGRG20.54

Disease biology

1 match

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Cystic fibrosis transmembrane conductance regulatorvia CFTR0.82

Reference

Authoritative identity, definition & identifiers.

Synonyms

CAVD, CBAVD, congenital bilateral absence of vas deferens, congenital bilateral aplasia of the vas deferens, vas deferens, congenital bilateral aplasia of

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.